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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508710Generated: October 26, 2026

4-Bromophenylhydrazine → 4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]aniline

https://huagongshe.com/reaction/508710

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenylhydrazineHCID 12158—
Reactant2-Chloro-6-fluorobenzaldehydeHCID 67847—
ReactantSodium BicarbonateHCID 516892—
SolventEthanolHCID 702—
Product4-bromo-N-[(E)-(2-chloro-6-fluorophenyl)methylideneamino]anilineHCID 9003365831.4%

Reaction Steps

To a solution of 2-chloro-6-fluorobenzaldehyde (1.0 g, 6.32 mmol) in ethanol was added (4-bromophenyl)hydrazine (1.7 g, 7.59 mmol) and aq. solution of NaHCO3 (0.637 g, 4.59 mmol). The reaction mixture was stirred at RT for 5-6 h. The reaction mass was quenched in water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated. The obtained crude product was purified by column chromatography on silica gel, eluting with 4.6% EA: pet. ether to afford 0.650 g of the desired product. 1H NMR (300 MHz, DMSO d6): δ 6.98 (d, J=7.8 Hz, 2H), 7.23-7.40 (m, 5H), 8.07 (s, 1H), 10.87 (br s, 1H). MS (m/z): 329.17 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096545B2
Source datasetuspto-grants-2015_08
ORD IDord-1f5e3475cc4e498981b286f562f98842
Source noteuspto-grants-2015_08